Anspach Effort Recalls Autolube-III Pneumatic Systems Due to Missing Service Interval
The Anspach Effort, Inc. is recalling 16 Autolube-III pneumatic systems because the supplied directions for use did not contain a recommended service interval.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class II, but the specific defect is a documentation issue (missing service interval in the Directions for Use) with no reported injuries or illnesses, fitting the criteria for a Low severity score (documentation issues).
Plain-English summary
The Anspach Effort, Inc. is recalling 16 units of the Autolube-III with 20ft hose, a pneumatic system. The recall was initiated because the supplied Directions for Use (DFU) did not contain a recommended service interval.
The affected products were distributed worldwide, including in the United States (specifically Hawaii and the District of Columbia), Puerto Rico, Guam, and Japan. The recall covers all product shipped prior to September 27, 2016, identified by DFU 18-0040 and Part No. AUTOLUBE-III-20.
Consumers who possess this product should stop using it and contact The Anspach Effort, Inc. for further instructions.
The recalled product
- Product
- Autolube-III with 20ft hose Product Usage: Pneumatic system
- Manufacturer
- The Anspach Effort, Inc.
- Hazard
- Affected units
- 16
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- All product shipped prior to 09/27/2016
- DFU 18-0040
- Part No. AUTOLUBE-III-20
Distribution
Part of a larger recall action
This product is one of 103 recalled by The Anspach Effort, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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